A highly selective sample cleanup procedure combined with molecularly imprinted solid-phase extraction (MISPE) was developed for the isolation of gonyautoxins 2,3 (GTX2,3) from Alexandrium tamarense sample. The molecularly imprinted polymer microspheres (MIPMs) were prepared by suspension polymerization using caffeine as the dummy template molecule, methacrylic acid as the functional monomer, ethylene glycol dimethacrylate as the cross-linker and polyvinyl alcohol as the dispersive reagent. The polymer microspheres were used as a selective sorbent for the solid-phase extraction of gonyautoxins 2,3. An off-line MISPE method followed by high-performance liquid chromatography (HPLC) with fluorescence detection for the analysis of gonyautoxins 2,3 was established. Finally, the extract samples from Alexandrium tamarense were analyzed. The results showed the imprinted polymer microspheres exhibited high affinity and selectivity for gonyautoxins 2,3. The interference matrix in the extract were obviously cleaned by MISPE and the extraction efficiency of gonyautoxins 2,3 in the sample ranged from 81.74% to 85.86%.

Carbon disulfide (CS₂) is seen an odor-toxic organic sulfur compound, which presents a major impact on global climate change. Therefore, the conversion of CS₂ into valuable chemicals is the key to reduce the concentration of CS₂ in the atmosphere. On the basis of a CS₂ fixation strategy, CS₂-storage materials (CS₂SMs) are firstly synthesized by the reaction of CS₂ with a binary ion-like liquid systems of ethylenediamine (EDA) and ethylene glycol derivatives (EGs) under mild condition. In view of the serious shortage of sulfur fertilizer and its important position in global agricultural production, it is a promising choice to use the CS₂SMs as a new type of green sulfur fertilizer to promote the growth of eggplant, tomato, sweet pepper and cucumber. In this work, the influence of CS₂SMs on the growth of plants were studied by taking plants irrigated by using various aqueous CS₂SMs solutions as experimental groups, and those irrigated by using water and NH₄HCO₃ as control groups. The experimental results showed that all CS₂SMs could promote plant height, stem diameter, root weight, flower bud number and leaf size. Especially, several CS₂SMs presented significant influence on fluorescence and fruit number. Further studies showed that the CS₂SMs as new energy resources sulfur-containing boosted leaf area, improved root development, enhanced photosynthesis and soil nutrient uptake, and promoted vegetative and reproductive growth of these four types of plants. Thus, this work provided a new strategy for the use of CS₂ as an indirect energy source for the experimental four plants.

Many surface and ground waters in the continental US are contaminated with a variety of chemical pollutants, which are usually present in concentrations in the ppm and ppb range. The effects of these pollutants on coliform bacteria, which are prominent members of the aquatic flora, are poorly understood. Using a microtiter plate assay, isolates of Escherichia coli (from chicken intestine and fresh water), and an isolate of Klebsiella pneumoniae (from bovine milk) were exposed to varying concentrations of common pollutants over a 24 h period. The herbicides/pesticides simazine, atrazine, and diazinon; the VOCs trichloroethene and MTBE; the estrogens estradiol and estrone; and caffeine, all failed to inhibit bacterial growth at ppm levels. Only ethylene glycol, and the herbicide 2,4-D, significantly inhibited bacterial growth compared to controls. These results suggest that the replication of coliform bacteria in fresh waters is not adversely impacted by many common pollutants. Using a microtiter plate assay, E. coli and Klebsiella bacteria were exposed to a panel of common chemical pollutants of fresh water; only ethylene glycol and 2,4-D inhibited bacterial replication.

A high selective pre-treatment method for the extraction and analysis of mebendazole in environmental water samples was developed based on molecularly imprinted solid-phase extraction (MISPE). The mebendazole imprinted polymers were synthesized in acetonitrile using methacrylic acid and ethylene glycol dimethacrylate as functional monomer and cross-linker respectively. The imprinted materials showed high adsorption ability for mebendazole and were applied as special solid-phase extraction sorbents for selective separation of mebendazole. An off-line MISPE procedure was developed for the purification and enrichment of mebendazole from natural seawater samples prior to high-performance liquid chromatography analysis. The recoveries of spiked seawater on the MISPE cartridges were from 83.0% to 90.6%, and the values of the relative standard deviation were in the range of 2.78–4.13% (n=3). The satisfied results showed that this pre-treatment methodology for extracting mebendazole in seawater was simple and effective.

An effective 3-step method for the quantification of mass of polyethylene terephthalate microplastics and nanoplastics (PET MNPs) in complex environmental matrices was developed based on a simplified in-matrix depolymerization. Liquid chromatography (LC) coupled with ultraviolet (UV) detection was used for detection and quantification. Recoveries for PET-spiked sand samples were 99 ± 2% (1 mg/L) and 93 ± 7% (30 mg/L). The limit of quantification (LOQ) for PET was 0.4 μg/g for sand, 1 mg/g for indoor dust and 0.2 μg/g for wet sludge. This method was applied to seven beach sand samples, 20 indoor dust samples and one sewage sludge sample. PET MNPs levels in sand samples were all below the limit of detection (LOD) of LC-UV (0.1 μg/g). The concentrations of PET MNPs in indoor dust samples ranged from 1.2 to 305 mg/g and the PET MNPs in liquid sludge was 1.5 mg/L.

In this paper, a highly selective sample cleanup procedure combining molecular imprinting technique (MIT) and solid-phase extraction (SPE) was developed for the isolation of malachite green in seawater and seafood samples. The molecularly imprinted polymer (MIP) was prepared using malachite green as the template molecule, methacrylic acid as the functional monomer and ethylene glycol dimethacrylate as the cross-linking monomer. The imprinted polymer and non-imprinted polymer were characterized by scanning electron microscope and static adsorption experiments. The MIP showed a high adsorption capacity and was used as selective sorbent for the SPE of malachite green. An off-line molecularly imprinted solid-phase extraction (MISPE) method followed by high-performance liquid chromatography with diodearray detection for the analysis of malachite green in seawater and seafood samples was also established. Finally, five samples were determined. The results showed that malachite green concentration in one seawater sample was at 1.30μgL⁻¹ and the RSD (n=3) was 4.15%.

The present study aimed to investigate the persistence and existence of chemical warfare agents (CWAs) and related dissipation products in the environment of Sardasht area, Iran. Three types of environmental samples including water, soil, and native local plant materials were collected and analyzed. Gas chromatography-mass spectrometry in the electron impact ionization mode has been developed for the separation, screening, identification, and qualification of chemicals after the sample preparation methods. The initial results revealed that no trace of related compounds or CWAs was detected in the soil and water samples. However, trace amounts of some degradation products of blistering agents like mustard gas (HD) and lewisite were found in a tree wood from a house subjected to chemical attack as well as in barley samples (a mixture of leaves and root) collected from an agricultural field in the area indicating chronic low exposure to the environment and people. In order to validate the applied extraction procedures, ethylene glycol was spiked to some of the samples including groundwater, surface soil, grape, and alfalfa plants. All the recoveries were in the range of 83.6–107.4% with the relative standard deviations varying from 4.9% to 12.4% (n = 3) successfully.

Previous studies have shown insufficient dispersion and thermal stability of nanofluids for high-temperature carbon capture and storage applications. Compared to the other NPs, TiO₂ nanofluids exhibit superior stability due to their high zeta potential. In previous studies, TiO₂ nanofluids have shown superior performance in heat transfer and cooling applications along with importing the stability of other nanofluids like SiO₂ in form of nanocomposites. Therefore, in this study, a nanofluid formulation consisting of titania nanofluid in a base solution of ethylene glycol (EG) with different co-stabilizers such as surfactants was synthesized for better dispersion stability, enhanced electrical, and rheological properties especially for the use in high-temperature industrial applications which include carbon capture and storage along with enhanced oil recovery. The formulated nanofluid was investigated for stability using dynamic light scattering (DLS) study and electrical conductivity. Additionally, the formulated nanofluid was also examined for thermal stability at high temperatures using an electrical conductivity study followed by rheological measurements at 30 and 90 °C. At a high temperature, the shear-thinning behavior of EG was found highly affected by shear rate; however, this deformation was controlled using TiO₂ nanoparticles (NPs). Furthermore, the role of surfactant was also investigated on dispersion stability, electrical conductivity followed by viscosity results, and it was found that the nanofluid is superior in presence of anionic surfactant sodium dodecyl sulfate (SDS) as compared to nonionic surfactant Triton X-100 (TX-100). The inclusion of ionic surfactant provides a charged layer of micelles surrounding the core of a NP and it produced additional surface potential. Consequently, it increases the repulsive force between two adjacent NPs and renders a greater stability to nanofluid while nonionic surfactant allowed monomers to adsorb on the surface of NP via hydrophobic interaction and enhances the short-range interparticle repulsion, to stabilize nanofluid. This makes titania nanofluid suitable for widespread high-temperature applications where conventional nanofluids face limitations. Finally, the application of the synthesized titania nanofluids was explored for the capture and transport of CO₂ where the inclusion of the anionic surfactant was found to increase the CO₂ capturing ability of titania nanofluids by 140–220% (over the conventional nanofluid) while also showing superior retention at both investigated temperatures. Thus, the study promotes the role of novel surfactant-treated titania nanofluids for carbon removal and storage and recommends their applications involving carbonated fluid injection (CFI) to carbon utilization in oilfield applications.

Wastewater samples originating from an explosives production plant (3,000 mg N l−1 nitrate, 4.8 mg l−1 nitroglycerin, 1.9 mg l−1 nitroglycol and 1,200 mg l−1 chemical oxygen demand) were subjected to biological purification. An attempt to completely remove nitrate and to decrease the chemical oxygen demand was carried out under anaerobic conditions. A soil isolated microbial consortium capable of biodegrading various organic compounds and reduce nitrate to atmospheric nitrogen under anaerobic conditions was used. Complete removal of nitrates with simultaneous elimination of nitroglycerin and ethylene glycol dinitrate (nitroglycol) was achieved as a result of the conducted research. Specific nitrate reduction rate was estimated at 12.3 mg N g−1 VSS h−1. Toxicity of wastewater samples during the denitrification process was studied by measuring the activity of dehydrogenases in the activated sludge. Mutagenicity was determined by employing the Ames test. The maximum mutagenic activity did not exceed 0.5. The obtained results suggest that the studied wastewater samples did not exhibit mutagenic properties.

In this study, nanoporous anodic film was produced by anodization of niobium, Nb in a fluoride ethylene glycol electrolyte. The effect of anodization voltage and electrolyte temperature was studied to find an optimum condition for circular, ordered, and uniform pore formation. The diameter of the pores was found to be larger when the applied voltage was increased from 20 to 80 V. The as-anodized porous film was also observed to comprise of nanocrystallites which formed due to high field-induced crystallization. The nanocrystallites grew into orthorhombic Nb₂O₅ after post-annealing treatment. The Cr(VI) photoreduction property of both the as-anodized and annealed Nb₂O₅ samples obtained using an optimized condition (anodization voltage: 60 V, electrolyte temperature: 70 °C) was compared. Interestingly, the as-anodized Nb₂O₅ film was found to display better photoreduction of Cr(VI) than annealed Nb₂O₅. However, in terms of stability, the annealed Nb₂O₅ presented high photocatalytic efficiency for each cycle whereas the as-anodized Nb₂O₅ showed degradation in photocatalytic performance when used continually.